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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1171903Erstellt: 25. Oktober 2026

Formaldehyde → HCID 23627568, Verbindung

https://huagongshe.com/reaction/1171903

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt(S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazineHCID 16725642—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 23627568HCID 2362756891%

Reaktionsschritte

A solution of (S)-3-Benzyl-1-(3-cyclopentyloxy-4-methoxy-phenyl)-piperazine (Example 2) (73 mg, 0.2 mmol) in CH2Cl2 (5 mL) was treated with a 37% aqueous formaldehyde solution (16.4 uL, 0.22 mmol) and stirred for 5 min after which time solid sodium triacetoxyborohydride (64 mg, 0.3 mmol) was added. The suspension was then stirred for 3 hr then quenched with a saturated aqueous NaHCO3 solution (2 mL). The organic component was separated, dried over MgSO4, filtered, and evaporated to an oil which was purified by silica gel flash chromatography with 5% MeOH/CH2Cl2 as eluant to afford product as a burgundy oil (69 mg, 91%). 1H NMR (CDCl3) 1.54-1.61 (m, 2H), 1.77-1.85 (m, 6H), 2.57 (s, 3H), 2.60-2.67 (m, 3H), 3.02-3.13 (m, 3H), 3.22-3.32 (m, 2H), 3.76 (s, 3H), 4.59-4.62 (m, 1H), 3.76 (s, 3 H), 4.59-4.62 (m, 1H), 6.30 (dd, J=8.6, 2.9, 1H), 6.35 (d, J=8.6, 1H), 7.20-7.33 (m, 5H). 13C NMR 24.2 (CH2), 33.0 (CH2), 36.3 (CH2), 42.9(CH3), 50.2 (CH2), 55.0 (CH2), 55.1 (CH2), 56.8 (CH3), 63.7 (CH), 80.4 (CH), 106.2 (CH), 107.8(CH), 113.2(CH), 126.4 (CH) 128.6, 129.5 (CH), 139.0 (CH), 144.5, 146.1, 148.4. LC/MS 5.10 min, [M+1]+ 381.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07829713B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-403e95c19c0a401ebe3bb4105e163d15
Quellennotizuspto-grants-2010_11